Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7578597 0.807 0.240 2 43505684 missense variant T/C snv 9.9E-02 0.14 2
rs10203174 1.000 0.080 2 43462891 intron variant C/T snv 0.17 1
rs11899863 1.000 0.080 2 43391680 intron variant C/T snv 8.5E-02 1